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2-(乙基硫代)-1H-苯并咪唑

更新时间:2025-09-12 10:14:21

2-(乙基硫代)-1H-苯并咪唑结构式
2-(乙基硫代)-1H-苯并咪唑结构式
品牌特惠专场
常用名 2-(乙基硫代)-1H-苯并咪唑 英文名 2-(Ethylthio)-1H-Benzo[d]Imidazole
CAS号 14610-11-8 分子量 178.25400
密度 N/A 沸点 N/A
分子式 C9H10N2S 熔点 N/A
MSDS N/A 闪点 N/A

 2-(乙基硫代)-1H-苯并咪唑名称

中文名 2-(乙基硫代)-(9ci)-1H-苯并咪唑
英文名 2-ethylsulfanyl-1H-benzimidazole
英文别名 更多

 2-(乙基硫代)-1H-苯并咪唑物理化学性质

分子式 C9H10N2S
分子量 178.25400
精确质量 178.05600
PSA 53.98000
LogP 2.67490
InChIKey UGCOPUIBNABIEP-UHFFFAOYSA-N
SMILES CCSc1nc2ccccc2[nH]1
储存条件 室温

 2-(乙基硫代)-1H-苯并咪唑安全信息

海关编码 2933990090

 2-(乙基硫代)-1H-苯并咪唑合成线路

~91%

2-(乙基硫代)-1H-苯并咪唑结构式

2-(乙基硫代)-1H-苯并咪唑

14610-11-8

文献:Dalal; Pawar; Mahulikar Organic Preparations and Procedures International, 2005 , vol. 37, # 6 p. 539 - 546

~0%

2-(乙基硫代)-1H-苯并咪唑结构式

2-(乙基硫代)-1H-苯并咪唑

14610-11-8

文献:Graber, David R.; Morge, Raymond A.; Sih, John C. Journal of Organic Chemistry, 1987 , vol. 52, # 20 p. 4620 - 4622

~86%

2-(乙基硫代)-1H-苯并咪唑结构式

2-(乙基硫代)-1H-苯并咪唑

14610-11-8

文献:Abramova, N. D.; Skvortsova, G. G.; Trzhtsinskaya, B. V. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1984 , vol. 20, # 6 p. 656 - 658 Khimiya Geterotsiklicheskikh Soedinenii, 1984 , vol. 20, # 6 p. 805 - 807

~%

2-(乙基硫代)-1H-苯并咪唑结构式

2-(乙基硫代)-1H-苯并咪唑

14610-11-8

文献:Journal of Organic Chemistry, , vol. 52, # 20 p. 4620 - 4622

~%

2-(乙基硫代)-1H-苯并咪唑结构式

2-(乙基硫代)-1H-苯并咪唑

14610-11-8

文献:Journal of the Chemical Society, , p. 452,456 Yakugaku Zasshi, , vol. 74, p. 1365,1367, 1368 Chem.Abstr., , p. 15876 Archiv der Pharmazie (Weinheim, Germany), , vol. 291, p. 113,114

 2-(乙基硫代)-1H-苯并咪唑海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 2-(乙基硫代)-1H-苯并咪唑靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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 2-(乙基硫代)-1H-苯并咪唑英文别名

2-ethylthiobenzimidazole
2-Ethylsulfanyl-1H-benzoimidazole
F1011-0541
2-Aethylmercapto-1H-benzimidazol
2-mercaptoethylbenzimidazole
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